Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck5 |
G |
A |
15: 76,478,383 (GRCm39) |
D277N |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,670,288 (GRCm39) |
S2353T |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,743,371 (GRCm39) |
N43K |
probably damaging |
Het |
Adnp2 |
A |
G |
18: 80,185,937 (GRCm39) |
I12T |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,741,363 (GRCm39) |
L903P |
probably damaging |
Het |
Ankhd1 |
T |
G |
18: 36,780,878 (GRCm39) |
S1977A |
probably benign |
Het |
Ap1m2 |
T |
C |
9: 21,216,983 (GRCm39) |
M118V |
probably benign |
Het |
Ap3d1 |
T |
C |
10: 80,548,639 (GRCm39) |
K846R |
possibly damaging |
Het |
Aqr |
C |
A |
2: 113,971,396 (GRCm39) |
E480* |
probably null |
Het |
Arl6 |
G |
T |
16: 59,434,199 (GRCm39) |
Q182K |
probably benign |
Het |
Arpc2 |
A |
G |
1: 74,294,034 (GRCm39) |
K106E |
probably benign |
Het |
Atp8a1 |
A |
C |
5: 67,889,524 (GRCm39) |
F599V |
|
Het |
B3galt5 |
A |
T |
16: 96,117,203 (GRCm39) |
I279F |
probably damaging |
Het |
Calcoco2 |
G |
T |
11: 95,991,104 (GRCm39) |
A211D |
unknown |
Het |
Ccdc33 |
T |
C |
9: 57,993,855 (GRCm39) |
E342G |
possibly damaging |
Het |
Cdh20 |
A |
G |
1: 104,862,065 (GRCm39) |
K82E |
probably benign |
Het |
Clca3a2 |
A |
T |
3: 144,503,575 (GRCm39) |
Y792N |
probably damaging |
Het |
Col6a6 |
T |
C |
9: 105,658,254 (GRCm39) |
I653V |
probably benign |
Het |
Col7a1 |
C |
T |
9: 108,812,649 (GRCm39) |
R2826W |
unknown |
Het |
D6Ertd527e |
A |
G |
6: 87,088,908 (GRCm39) |
N357S |
unknown |
Het |
Dmgdh |
T |
A |
13: 93,857,123 (GRCm39) |
N742K |
probably benign |
Het |
Dnai3 |
T |
C |
3: 145,748,594 (GRCm39) |
N840S |
probably benign |
Het |
Dnajc6 |
A |
G |
4: 101,475,821 (GRCm39) |
N565D |
probably benign |
Het |
Doc2g |
A |
G |
19: 4,054,390 (GRCm39) |
Y155C |
probably damaging |
Het |
Dot1l |
G |
A |
10: 80,624,361 (GRCm39) |
G943D |
probably damaging |
Het |
Dst |
T |
C |
1: 34,220,736 (GRCm39) |
V2180A |
probably benign |
Het |
Eftud2 |
A |
C |
11: 102,759,422 (GRCm39) |
Y160* |
probably null |
Het |
Ehd1 |
A |
T |
19: 6,331,262 (GRCm39) |
Q140L |
probably benign |
Het |
Etv3 |
T |
C |
3: 87,443,172 (GRCm39) |
V252A |
probably benign |
Het |
F11 |
A |
T |
8: 45,694,566 (GRCm39) |
C598* |
probably null |
Het |
Fancm |
T |
A |
12: 65,137,758 (GRCm39) |
N316K |
probably benign |
Het |
Flnc |
T |
C |
6: 29,457,214 (GRCm39) |
V2372A |
probably damaging |
Het |
Fry |
A |
G |
5: 150,282,488 (GRCm39) |
R338G |
probably damaging |
Het |
Gfra3 |
T |
C |
18: 34,837,591 (GRCm39) |
T136A |
probably benign |
Het |
Golga7b |
T |
C |
19: 42,255,462 (GRCm39) |
V113A |
possibly damaging |
Het |
Gpn3 |
G |
T |
5: 122,520,306 (GRCm39) |
V102L |
|
Het |
Herc2 |
A |
G |
7: 55,820,338 (GRCm39) |
N2859S |
possibly damaging |
Het |
Hpd |
A |
T |
5: 123,318,948 (GRCm39) |
|
probably null |
Het |
Hspg2 |
C |
T |
4: 137,266,887 (GRCm39) |
T1964I |
probably benign |
Het |
Hydin |
A |
T |
8: 111,220,965 (GRCm39) |
T1454S |
probably benign |
Het |
Irgm2 |
A |
T |
11: 58,110,872 (GRCm39) |
T188S |
possibly damaging |
Het |
Jak3 |
A |
G |
8: 72,131,366 (GRCm39) |
D77G |
probably damaging |
Het |
Kcnj4 |
G |
T |
15: 79,369,220 (GRCm39) |
F253L |
possibly damaging |
Het |
Kidins220 |
T |
A |
12: 25,106,895 (GRCm39) |
D1358E |
probably benign |
Het |
Klf1 |
C |
A |
8: 85,630,061 (GRCm39) |
C295* |
probably null |
Het |
Kmt2a |
C |
T |
9: 44,760,102 (GRCm39) |
W582* |
probably null |
Het |
Lrig2 |
A |
G |
3: 104,371,556 (GRCm39) |
C716R |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 40,765,004 (GRCm39) |
D2941N |
|
Het |
Lrpprc |
A |
T |
17: 85,020,262 (GRCm39) |
V1141E |
probably damaging |
Het |
Mrgprx1 |
C |
T |
7: 47,671,273 (GRCm39) |
G158D |
probably benign |
Het |
Muc5b |
C |
A |
7: 141,409,279 (GRCm39) |
A1121D |
unknown |
Het |
Nf1 |
G |
T |
11: 79,334,733 (GRCm39) |
V852L |
probably damaging |
Het |
Nlrp5 |
A |
G |
7: 23,118,286 (GRCm39) |
E670G |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,784,601 (GRCm39) |
T101A |
probably benign |
Het |
Or10a49 |
T |
C |
7: 108,467,563 (GRCm39) |
Y266C |
probably damaging |
Het |
Or2t35 |
T |
A |
14: 14,407,963 (GRCm38) |
I245K |
probably benign |
Het |
Or5b123 |
G |
A |
19: 13,597,365 (GRCm39) |
V237I |
probably benign |
Het |
P2rx2 |
T |
C |
5: 110,488,172 (GRCm39) |
T461A |
probably benign |
Het |
Pank1 |
G |
A |
19: 34,799,194 (GRCm39) |
T419I |
probably damaging |
Het |
Patz1 |
T |
C |
11: 3,244,562 (GRCm39) |
V481A |
unknown |
Het |
Pdlim5 |
A |
G |
3: 142,018,058 (GRCm39) |
L179P |
probably benign |
Het |
Pik3ap1 |
A |
T |
19: 41,296,967 (GRCm39) |
V461D |
probably damaging |
Het |
Polq |
T |
C |
16: 36,848,176 (GRCm39) |
V261A |
probably damaging |
Het |
Ppm1a |
G |
A |
12: 72,837,451 (GRCm39) |
V333M |
possibly damaging |
Het |
R3hcc1l |
T |
C |
19: 42,552,671 (GRCm39) |
L556P |
probably benign |
Het |
Rabggta |
G |
A |
14: 55,956,375 (GRCm39) |
Q365* |
probably null |
Het |
Ranbp9 |
T |
C |
13: 43,578,519 (GRCm39) |
T185A |
probably benign |
Het |
Rd3l |
T |
G |
12: 111,945,913 (GRCm39) |
N189H |
probably damaging |
Het |
Rnf17 |
A |
G |
14: 56,722,636 (GRCm39) |
T1066A |
probably damaging |
Het |
Rnf213 |
G |
A |
11: 119,332,794 (GRCm39) |
A2669T |
|
Het |
Ros1 |
T |
A |
10: 51,996,931 (GRCm39) |
H1268L |
probably benign |
Het |
Rps6ka4 |
G |
T |
19: 6,809,354 (GRCm39) |
S433R |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,759,092 (GRCm39) |
L3362P |
probably damaging |
Het |
Setd1b |
A |
T |
5: 123,298,046 (GRCm39) |
T1361S |
unknown |
Het |
Setd2 |
T |
C |
9: 110,377,570 (GRCm39) |
S462P |
probably damaging |
Het |
Sgsm3 |
A |
T |
15: 80,890,935 (GRCm39) |
Q132L |
probably benign |
Het |
Slx1b |
C |
A |
7: 126,291,698 (GRCm39) |
R122L |
probably damaging |
Het |
Sorbs2 |
A |
T |
8: 46,276,788 (GRCm39) |
T1167S |
probably benign |
Het |
Spdya |
A |
C |
17: 71,869,513 (GRCm39) |
T103P |
probably damaging |
Het |
Stfa2 |
A |
G |
16: 36,228,638 (GRCm39) |
S20P |
probably benign |
Het |
Sulf1 |
A |
G |
1: 12,891,026 (GRCm39) |
T400A |
probably benign |
Het |
Tardbp |
A |
T |
4: 148,709,751 (GRCm39) |
D23E |
probably damaging |
Het |
Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
Tgm1 |
C |
T |
14: 55,948,441 (GRCm39) |
D237N |
probably benign |
Het |
Tgs1 |
T |
A |
4: 3,585,964 (GRCm39) |
N280K |
probably benign |
Het |
Tmem198 |
A |
T |
1: 75,459,272 (GRCm39) |
I76F |
possibly damaging |
Het |
Trpv2 |
A |
T |
11: 62,475,385 (GRCm39) |
Y266F |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,569,845 (GRCm39) |
G27016E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,781,824 (GRCm39) |
E1074G |
unknown |
Het |
Unc5b |
A |
T |
10: 60,613,322 (GRCm39) |
W305R |
probably damaging |
Het |
Usp38 |
A |
G |
8: 81,741,164 (GRCm39) |
|
probably benign |
Het |
Vmn1r79 |
A |
G |
7: 11,910,582 (GRCm39) |
T155A |
probably benign |
Het |
Vwce |
G |
A |
19: 10,615,481 (GRCm39) |
V121I |
probably benign |
Het |
Wdr91 |
A |
T |
6: 34,865,961 (GRCm39) |
D530E |
probably benign |
Het |
Wnt4 |
A |
G |
4: 137,023,929 (GRCm39) |
T299A |
probably benign |
Het |
Yeats2 |
T |
A |
16: 20,047,491 (GRCm39) |
Y1284* |
probably null |
Het |
Zfp113 |
A |
T |
5: 138,148,888 (GRCm39) |
Y85* |
probably null |
Het |
Zfp184 |
A |
G |
13: 22,144,096 (GRCm39) |
T601A |
probably benign |
Het |
Zfp655 |
A |
G |
5: 145,180,442 (GRCm39) |
E100G |
probably damaging |
Het |
|
Other mutations in Ccdc88a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00499:Ccdc88a
|
APN |
11 |
29,449,341 (GRCm39) |
missense |
probably benign |
0.24 |
IGL00577:Ccdc88a
|
APN |
11 |
29,374,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00766:Ccdc88a
|
APN |
11 |
29,451,046 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01384:Ccdc88a
|
APN |
11 |
29,453,915 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01541:Ccdc88a
|
APN |
11 |
29,350,283 (GRCm39) |
missense |
probably benign |
|
IGL01647:Ccdc88a
|
APN |
11 |
29,454,321 (GRCm39) |
unclassified |
probably benign |
|
IGL02648:Ccdc88a
|
APN |
11 |
29,451,051 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02885:Ccdc88a
|
APN |
11 |
29,398,050 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03117:Ccdc88a
|
APN |
11 |
29,324,559 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03196:Ccdc88a
|
APN |
11 |
29,432,340 (GRCm39) |
missense |
possibly damaging |
0.56 |
trailor
|
UTSW |
11 |
29,444,099 (GRCm39) |
splice site |
probably null |
|
R0011:Ccdc88a
|
UTSW |
11 |
29,324,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Ccdc88a
|
UTSW |
11 |
29,324,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R0083:Ccdc88a
|
UTSW |
11 |
29,453,463 (GRCm39) |
missense |
probably damaging |
0.99 |
R0108:Ccdc88a
|
UTSW |
11 |
29,453,463 (GRCm39) |
missense |
probably damaging |
0.99 |
R0326:Ccdc88a
|
UTSW |
11 |
29,411,021 (GRCm39) |
missense |
probably benign |
0.01 |
R0565:Ccdc88a
|
UTSW |
11 |
29,411,042 (GRCm39) |
unclassified |
probably benign |
|
R0631:Ccdc88a
|
UTSW |
11 |
29,443,752 (GRCm39) |
missense |
probably damaging |
0.98 |
R0632:Ccdc88a
|
UTSW |
11 |
29,432,749 (GRCm39) |
unclassified |
probably benign |
|
R0762:Ccdc88a
|
UTSW |
11 |
29,413,112 (GRCm39) |
unclassified |
probably benign |
|
R0838:Ccdc88a
|
UTSW |
11 |
29,350,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R0946:Ccdc88a
|
UTSW |
11 |
29,406,509 (GRCm39) |
missense |
probably benign |
|
R1192:Ccdc88a
|
UTSW |
11 |
29,454,049 (GRCm39) |
missense |
possibly damaging |
0.45 |
R1500:Ccdc88a
|
UTSW |
11 |
29,432,713 (GRCm39) |
missense |
probably benign |
0.00 |
R1701:Ccdc88a
|
UTSW |
11 |
29,427,427 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1826:Ccdc88a
|
UTSW |
11 |
29,439,637 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1902:Ccdc88a
|
UTSW |
11 |
29,411,788 (GRCm39) |
missense |
probably benign |
0.07 |
R1903:Ccdc88a
|
UTSW |
11 |
29,411,788 (GRCm39) |
missense |
probably benign |
0.07 |
R2021:Ccdc88a
|
UTSW |
11 |
29,453,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R2023:Ccdc88a
|
UTSW |
11 |
29,413,546 (GRCm39) |
nonsense |
probably null |
|
R2284:Ccdc88a
|
UTSW |
11 |
29,444,099 (GRCm39) |
splice site |
probably null |
|
R3236:Ccdc88a
|
UTSW |
11 |
29,397,995 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3409:Ccdc88a
|
UTSW |
11 |
29,436,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R3410:Ccdc88a
|
UTSW |
11 |
29,436,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R3411:Ccdc88a
|
UTSW |
11 |
29,436,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Ccdc88a
|
UTSW |
11 |
29,398,033 (GRCm39) |
missense |
probably damaging |
0.98 |
R3620:Ccdc88a
|
UTSW |
11 |
29,380,227 (GRCm39) |
missense |
probably benign |
0.16 |
R4204:Ccdc88a
|
UTSW |
11 |
29,413,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R4515:Ccdc88a
|
UTSW |
11 |
29,432,651 (GRCm39) |
missense |
probably benign |
0.01 |
R4518:Ccdc88a
|
UTSW |
11 |
29,432,651 (GRCm39) |
missense |
probably benign |
0.01 |
R4519:Ccdc88a
|
UTSW |
11 |
29,432,651 (GRCm39) |
missense |
probably benign |
0.01 |
R4693:Ccdc88a
|
UTSW |
11 |
29,432,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R4705:Ccdc88a
|
UTSW |
11 |
29,372,586 (GRCm39) |
missense |
probably benign |
|
R4707:Ccdc88a
|
UTSW |
11 |
29,397,956 (GRCm39) |
missense |
probably benign |
|
R4732:Ccdc88a
|
UTSW |
11 |
29,435,906 (GRCm39) |
missense |
probably benign |
0.02 |
R4733:Ccdc88a
|
UTSW |
11 |
29,435,906 (GRCm39) |
missense |
probably benign |
0.02 |
R4734:Ccdc88a
|
UTSW |
11 |
29,432,720 (GRCm39) |
missense |
probably benign |
|
R4749:Ccdc88a
|
UTSW |
11 |
29,432,720 (GRCm39) |
missense |
probably benign |
|
R4817:Ccdc88a
|
UTSW |
11 |
29,410,907 (GRCm39) |
missense |
probably benign |
0.15 |
R4828:Ccdc88a
|
UTSW |
11 |
29,413,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R4979:Ccdc88a
|
UTSW |
11 |
29,432,133 (GRCm39) |
nonsense |
probably null |
|
R5288:Ccdc88a
|
UTSW |
11 |
29,448,416 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5373:Ccdc88a
|
UTSW |
11 |
29,413,409 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5374:Ccdc88a
|
UTSW |
11 |
29,413,409 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5401:Ccdc88a
|
UTSW |
11 |
29,413,279 (GRCm39) |
missense |
probably benign |
0.00 |
R5586:Ccdc88a
|
UTSW |
11 |
29,453,484 (GRCm39) |
missense |
probably benign |
0.00 |
R6660:Ccdc88a
|
UTSW |
11 |
29,432,663 (GRCm39) |
missense |
probably benign |
0.01 |
R7116:Ccdc88a
|
UTSW |
11 |
29,454,051 (GRCm39) |
missense |
probably benign |
0.01 |
R7353:Ccdc88a
|
UTSW |
11 |
29,413,368 (GRCm39) |
missense |
probably benign |
0.00 |
R7538:Ccdc88a
|
UTSW |
11 |
29,413,370 (GRCm39) |
missense |
probably benign |
0.00 |
R7663:Ccdc88a
|
UTSW |
11 |
29,448,614 (GRCm39) |
critical splice donor site |
probably null |
|
R7769:Ccdc88a
|
UTSW |
11 |
29,432,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R7798:Ccdc88a
|
UTSW |
11 |
29,427,348 (GRCm39) |
missense |
probably benign |
0.15 |
R7810:Ccdc88a
|
UTSW |
11 |
29,435,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R7826:Ccdc88a
|
UTSW |
11 |
29,453,563 (GRCm39) |
missense |
probably benign |
0.02 |
R7956:Ccdc88a
|
UTSW |
11 |
29,413,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R8260:Ccdc88a
|
UTSW |
11 |
29,443,934 (GRCm39) |
missense |
probably benign |
0.01 |
R8402:Ccdc88a
|
UTSW |
11 |
29,413,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R8409:Ccdc88a
|
UTSW |
11 |
29,453,544 (GRCm39) |
missense |
probably benign |
|
R8555:Ccdc88a
|
UTSW |
11 |
29,380,169 (GRCm39) |
missense |
probably benign |
|
R8676:Ccdc88a
|
UTSW |
11 |
29,410,860 (GRCm39) |
missense |
probably benign |
0.05 |
R8846:Ccdc88a
|
UTSW |
11 |
29,414,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Ccdc88a
|
UTSW |
11 |
29,448,416 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8972:Ccdc88a
|
UTSW |
11 |
29,435,888 (GRCm39) |
missense |
probably benign |
0.07 |
R9353:Ccdc88a
|
UTSW |
11 |
29,427,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R9362:Ccdc88a
|
UTSW |
11 |
29,453,922 (GRCm39) |
missense |
probably null |
0.55 |
R9385:Ccdc88a
|
UTSW |
11 |
29,405,422 (GRCm39) |
missense |
probably benign |
0.24 |
R9509:Ccdc88a
|
UTSW |
11 |
29,414,143 (GRCm39) |
missense |
probably benign |
0.27 |
R9610:Ccdc88a
|
UTSW |
11 |
29,427,316 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9611:Ccdc88a
|
UTSW |
11 |
29,427,316 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9720:Ccdc88a
|
UTSW |
11 |
29,413,813 (GRCm39) |
missense |
probably benign |
|
|